Product Wiki · Recalls · Health Canada — Medical Devices

Leksell GammaPlan® — recall 81399

Health Canada — Medical Devices · Canada · 2025-12-23 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
81399
Date of alert
2025-12-23
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Radiology
Product type
Medical devices
Reported risk: Defining a new stereotactic reference for a frame treatment without first changing an existing obsolete reference to a pre-plan reference may create inconsistent alignment and, if not detected, lead to irradiation of the wrong patient location.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/leksell-gammaplanr

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